Author(s): Nuning Rahmawati, Agung E. Nugroho, Yuli Widiyastuti, Abdul Rohman

Email(s): abdul_kimfar@ugm.ac.id

DOI: 10.52711/0974-360X.2026.00291   

Address: Nuning Rahmawati1,2, Agung E. Nugroho3, Yuli Widiyastuti2, Abdul Rohman4,5*
1Doctoral Graduate Program, Faculty of Pharmacy, Universitas Gadjah Mada, Yogyakarta 55281, Indonesia.
2Research Center for Pharmaceutical Ingredients and Traditional Medicine, National Research and Innovation Agency, Cibinong, West Java 16911, Indonesia.
3Department of Pharmacology and Clinical Pharmacy, Faculty of Pharmacy, Universitas Gadjah Mada, Yogyakarta 55281, Indonesia.
4Department of Pharmaceutical Chemistry, Faculty of Pharmacy, Universitas Gadjah Mada, Yogyakarta 55281, Indonesia.
5Center of Excellence, Institute for Halal Industry and Systems (PUI-PT IHIS UGM), Universitas Gadjah Mada, Indonesia.
*Corresponding Author

Published In:   Volume - 19,      Issue - 5,     Year - 2026


ABSTRACT:
Cananga odorata (Lam.) Hook.f. and Thomson (CO) is a good source of bioactive phytochemicals including phenolics, flavonoids, and saponins contributing to some biological activities needed for human health such as antidiabetic and antioxidant. The objective of this study was to evaluate the antidiabetic and antioxidant activities of Cananga odorata forma fruticosa (shrub Cananga), Cananga odorata forma macrophylla (Javanese Cananga), and Cananga odorata forma genuina (ylang-ylang) and its association with flavonoid and phenolics levels. The ethanolic extracts of CO leaves were subjected to the antidiabetic activities through the inhibitions of dipeptidyl peptidase 4(DPP-4) and a-glucosidase enzymes, while antioxidant activities were evaluated using 2,2- diphenyl-1-picrylhydrazyl (DPPH) radical scavenging and ferric reducing activity power (FRAP) methods. The levels of total phenolics and flavonoid contents were determined spectrophotometrically and correlated with the antidiabetic and antioxidant activities. The study showed that among three forma, Javanese Cananga exhibited the strongest inhibition activities toward a-glucosidase and DPP-4 enzymes, nonetheless, the results were lesser compared to the activities of positive controls of acarbose and sitagliptin. This forma has also revealed the highest antioxidant activities with IC50 of DPPH radical assay and FRAP value of 47.93±0.99µg/mL and 724.30±5.38, respectively. Loading plot of principle component analysis results demonstrate a positive association between phenolic content, DPPH, FRAP, DPP-4, and a-glucosidase of shrub Cananga, Javanese Cananga, and ylang-ylang. The study's findings highlighted the most prominent antidiabetic and antioxidant activity, together with the phenolic and flavonoid levels in Javanese Cananga rather than ylang-ylang and shrub Cananga. Hence, CO leaves extract of three forma can potentially be used as an antioxidants and anti-diabetic agent to avert and regulate oxidative stress and glucose levels.


Cite this article:
Nuning Rahmawati, Agung E. Nugroho, Yuli Widiyastuti, Abdul Rohman. Antidiabetic Effect, Antioxidant Potency, Phenolic and Flavonoid Content of Shrub Cananga, Javanese Cananga and Ylang-ylang and its Correlation with Chemometrics. Research Journal Pharmacy and Technology. 2026;19(5):2031-8. doi: 10.52711/0974-360X.2026.00291

Cite(Electronic):
Nuning Rahmawati, Agung E. Nugroho, Yuli Widiyastuti, Abdul Rohman. Antidiabetic Effect, Antioxidant Potency, Phenolic and Flavonoid Content of Shrub Cananga, Javanese Cananga and Ylang-ylang and its Correlation with Chemometrics. Research Journal Pharmacy and Technology. 2026;19(5):2031-8. doi: 10.52711/0974-360X.2026.00291   Available on: https://www.rjptonline.org/AbstractView.aspx?PID=2026-19-5-12


REFERENCES:
1.    Rates SMK. Plants as source of drugs. Toxicon. 2001; (39): 603–613. https://doi.org/10.1016/S0041-0101(00)00154-9.
2.    Sholikhah EN. Indonesian medicinal plants as sources of secondary metabolites for pharmaceutical industry. J Thee Med Sci (Berkala Ilmu Kedokteran). 2016; (48): 226–239. https://doi.org/10.19106/jmedsci004804201606.
3.    Jin J. Kim MJ. Dhandapani S. Tjhang JG. Yin JL. Wong L. The floral transcriptome of ylang ylang (Cananga odorata var. fruticosa) uncovers biosynthetic pathways for volatile organic compounds and a multifunctional and novel sesquiterpene synthase. J Exp Bot. 2015; (66): 3959–3975. https://doi.org/10.1093/jxb/erv196.
4.    Nurhayani FO. Wulandari AS. Suharsi TK. The Floral Morphology and Anatomy of Kenanga (Cananga odorata (Lam.) Hook.f. and Thomson). IOP Conf Ser Earth Environ Sci. 2019; (394). https://doi.org/10.1088/1755-1315/394/1/012034.
5.    Nurhayani FO. Wulandari AS. Suharsi TK. Morphology and anatomy of the fruit and seed of Cananga odorata (lam.) hook.f. and Thomson. Biodiversitas. 2019; (20): 3199–3206. https://doi.org/10.13057/biodiv/d201112.
6.    Mansur . Sari R. Response of Ylang-Ylang Seed Growth (Cananga odorata forma genuina) to Giving Leaf Fertilizers in Nursery. Silvikultur Trop. 2021;(12):102–108.
7.    Mrani SA. Zejli H. Azzouni D. Fadili D. Alanazi MM. Omar S. Chemical Composition, Antioxidant, Antibacterial, and Hemolytic Properties of Ylang-Ylang (Cananga odorata) Essential Oil : Potential Therapeutic Applications in Dermatology. Pharm 2024,. 2024; (17): 1–13.
8.    Borgonetti V. López V. Galeotti N. Ylang-ylang (Cananga odorata (Lam.) Hook. f. and Thomson) essential oil reduced neuropathic-pain and associated anxiety symptoms in mice. J Ethnopharmacol. 2022; (294). https://doi.org/10.1016/j.jep.2022.115362.
9.    Tan LTH. Lee LH. Yin WF. Chan CK. Abdul KH. Chan KG. Traditional uses, phytochemistry, and bioactivities of Cananga odorata (ylang-ylang). Evidence-Based Complement Altern Med. 2015; (2015). https://doi.org/10.1155/2015/896314.
10.    de Freitas JRA. Lossavaro PK de MB. Kassuya CAL. Paredes-Gamero EJ. Farias JNC. Souza MIL. Effect of Ylang-Ylang (Cananga odorata Hook. F. and Thomson) Essential Oil on Acute Inflammatory Response In Vitro and In Vivo. Molecules. 2022; (27): 3666. https://doi.org/10.3390/molecules27123666.
11.    Praparatana R. Maliyam P. Barrows LR. Puttarak P. Flavonoids and Phenols, the Potential Anti-Diabetic Compounds from Bauhinia strychnifolia Craib. Stem. Molecules. 2022; (27): 1–16. https://doi.org/10.3390/molecules27082393.
12.    Rohman A. Putri AR. The chemometrics techniques in combination with instrumental analytical methods applied in Halal authentication analysis. Indones J Chem. 2019; (19): 262–272. https://doi.org/10.22146/ijc.28721.
13.    Mistriyani. Riyanto S. Rohman A. Antioxidant activities of rambutan (Nephelium lappaceum L) peel in vitro. Food Res. 2018; (2): 119–123. https://doi.org/10.26656/fr.2017.2(1).150.
14.    Conget I. Diagnosis, Classification and Pathogenesis of Diabetes Mellitus. Rev Esp Cardiol. 2002; (55): 528–563.
15.    Rehani PR. Iftikhar H. Nakajima M. Tanaka T. Jabbar Z. Rehani RN. Safety and Mode of Action of Diabetes Medications in comparison with 5-Aminolevulinic Acid (5-ALA). J Diabetes Res. 2019; (2019). https://doi.org/10.1155/2019/4267357.
16.    Gondokesumo ME. Muslikh FA. The Effect of Keluwih (Artocarpus camansi) Leaves Extract On Pro-Inflammatory Expression, Growth Factors and Bodies in Zebrafish Larvae (Danio rerio) Stunting Model. Biomed Pharmacol J. 2024; (17): 1647–1653. https://doi.org/10.13005/bpj/2972.
17.    Nematollahi M. Taleb AM. Seyyed-Tabaei SJ. Ahmadi N. Leishmanicidal Activity and Cytotoxicity of Thymus kotschyanus Hydroalcoholic Extract: an In Vitro Assessment. Res J Pharmacogn. 2024; (11): 1–8. https://doi.org/10.22127/rjp.2024.445261.2369.
18.    Cicco N. Lanorte MT. Paraggio M, Viggiano M. Lattanzio V. A reproducible, rapid and inexpensive Folin-Ciocalteu micro-method in determining phenolics of plant methanol extracts. Microchem J. 2009; (91): 107–110. https://doi.org/10.1016/j.microc.2008.08.011.
19.    Widodo H. Sismindari S. Asmara W. Rohman A. Antioxidant activity, total phenolic and flavonoid contents of selected medicinal plants used for liver diseases and its classification with chemometrics. J Appl Pharm Sci. 2019; (9): 99–105. https://doi.org/10.7324/JAPS.2019.90614.
20.    Sharma OP. Bhat TK. DPPH antioxidant assay revisited. Food Chem. 2009; (113): 1202–1205. https://doi.org/10.1016/j.foodchem.2008.08.008.
21.    Benzie IFF. Strain JJ. The ferric reducing ability of plasma (FRAP) as a measure of “antioxidant power”: The FRAP assay. Anal Biochem. 1996; (239): 70–76. https://doi.org/10.1006/abio.1996.0292.
22.    Cáceres M. Hidalgo W. Stashenko EE. Torres R. Ortiz C. Maniyar YA. Insecticidal activity of two essential oils used in perfumery (ylang ylang and frankincense). Evidence-Based Complement Altern Med. 2021; (35): 1–10. https://doi.org/10.1016/j.apjtb.2017.01.025.
23.    Lawrence GH. An Introduction to Plant Taxonomy. Bull Torrey Bot Club. 1983;(110):231. https://doi.org/10.2307/2996350.
24.    Benini C. Mahy G. Bizoux JP. Wathelet JP. Du Jardin P. Brostaux Y. Comparative chemical and molecular variability of cananga odorata (Lam.) Hook.f. and thomson forma genuina (Ylang-Ylang) in the western indian ocean islands: Implication for valorization. Chem Biodivers. 2012; (9): 1389–1402. https://doi.org/10.1002/cbdv.201100306.
25.    Chris P. Orlando P. Christian P. Nutrient Content in Ylang-Ylang (Cananga odorata (Lam.) Hook.f. and Thoms., Annonaceae) Cultivated in Ecuador. Agrivita. 2023; (45): 613–620.
26.    Mahabir R. Maharaj S. Watson MJ. McGaw DR. Coonai C. Supercritical Extraction of Ylang Ylang (Cananga odorata) Essential Oil at the Near-Critical Region. Separations. 2024; (11): 1–10. https://doi.org/10.3390/separations11100295.
27.    Nugraheni YMMA, Mansur I, Sulistiani E. In vitro sterilization and callus induction from Cananga odorata forma genuina steenis explants. IOP Conf Ser Earth Environ Sci. 2023; (1192): 012017. https://doi.org/10.1088/1755-1315/1192/1/012017.
28.    Mallavarapu GR. Gurudutt KN. Syamasundar KV. Ylang-Ylang (Cananga odorata) Oils. Elsevier Inc.; 2016. https://doi.org/10.1016/B978-0-12-416641-7.00099-7.
29.    Benini C. Ringuet M. Wathelet JP. Lognay G. du Jardin P. Fauconnier ML. Variations in the essential oils from ylang-ylang (Cananga odorata [Lam.] Hook f. and Thomson forma genuina) in the Western Indian Ocean islands. Flavour Fragr J. 2012; (27): 356–366. https://doi.org/10.1002/ffj.3106.
30.    Chakira A. Garcia C. Soria C. Minier J. Chillet M. Effect of Flower Development Stages on the Dynamics of Volatile Compounds in Ylang-Ylang (Cananga odorata) Essential Oil. Horticulturae. 2022; (8). https://doi.org/10.3390/horticulturae8110986.
31.    Zhang Y. Liu J. Li J. Sun J. Liang B. Min X et al. betulinic acid derivatives as α -glucosidase inhibitors. J Mol Struct. 2025; (1328): 141252. https://doi.org/10.1016/j.molstruc.2024.141252.
32.    Pan J. Zhang Q. Zhang C. Yang W. Liu H. Lv Z et al. Inhibition of Dipeptidyl Peptidase-4 by Flavonoids: Structure–Activity Relationship, Kinetics and Interaction Mechanism. Front Nutr. 2022; (9): 1–17. https://doi.org/10.3389/fnut.2022.892426.
33.    Pechmann LM. Pinheiro FI. Andrade VFC. Moreira CA. The multiple actions of dipeptidyl peptidase 4 (DPP-4) and its pharmacological inhibition on bone metabolism: a review. Diabetol Metab Syndr. 2024; (16): 1–21. https://doi.org/10.1186/s13098-024-01412-x.
34.    Kristiawan M. Sobolik V. Allaf K. Isolation of Indonesian cananga oil using multi-cycle pressure drop process. J Chromatogr A. 2008; (1192): 306–318. https://doi.org/10.1016/j.chroma.2008.03.068.
35.    Ahalya SP. Vijayakumar T. Satish Kumar RC. Network pharmacological analysis of drug-drug interactions between glimepiride and phytochemicals in chandraprabha vati: Identifying common targets and molecular mechanism. J Med Pharm Chem Res. 2025; (7): 1676–1684. https://doi.org/10.48309/jmpcr.2025.480113.1443.
36.    Siddique NA. Antioxidant and antimicrobial potential of Delphinium denudatum Wall. Evaluated by validated high-performance thin-layer chromatography and in vitro assays. Kuwait J Sci. 2025; (52). https://doi.org/10.1016/j.kjs.2024.100352.
37.    Allouache R. Ben Haj Koubaier H. Mahmoudi I. Turki M. Snoussi A. Tunisian persimmon (Diospyros kaki L.) jelly: Effect on physicochemical, microbiological, rheological, biological activities and sensory properties of bilayer yogurt. Acta Sci - Technol. 2025; (47): 1–8. https://doi.org/10.4025/actascitechnol.v47i1.70534.
38.    Irshad A. Jawad R. Mushtaq Q. Spalletta A. Martin P. Ishtiaq U. Determination of antibacterial and antioxidant potential of organic crude extracts from Malus domestica, Cinnamomum verum and Trachyspermum ammi. Sci Rep. 2025; (15): 1–12. https://doi.org/10.1038/s41598-024-83506-0.
39.    Shukla R. Arya G. Sathyanarayana P. Antioxidant Activity Screening Models and Their Mechanism: a Review. Plant Arch. 2021; (21): 1024–1032. https://doi.org/10.51470/plantarchives.2021.v21.no1.111.
40.    Parhizkar T, Rafieipour E, Parhizkar A. Evaluation and improvement of energy consumption prediction models using principal component analysis based feature reduction. J Clean Prod. 2021; (279). https://doi.org/10.1016/j.jclepro.2020.123866.

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